Evidence map›Paper›PMID 41444553›Full record

ArticleBMC neurology2025

Etiologies of patients with adult-onset epilepsy over the past 25 years: a retrospective study in China.

Xu Zhang, Ziyu Wang, Feng Xiang, Yang Li, Xiaobing Shi, Chenjing Shao, Senyang Lang, Xiangqing Wang

Abstract read
In one paragraph

Article in BMC neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Xu Zhang *Department of Neurology, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Ziyu Wang *Department of Neuroelectrophysiology, Beijing Jishuitan Hospital, Capital Medical University, Beijing, China.
Feng XiangDepartment of Neurology, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Yang LiDepartment of Neurology, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Xiaobing ShiDepartment of Neurology, The Second Medical Center of Chinese PLA General Hospital, Beijing, China.
Chenjing ShaoDepartment of Gerontology, Beijing Jishuitan Hospital, Capital Medical University, Beijing, China.
Senyang LangDepartment of Neurology, Hainan Hospital of Chinese PLA General Hospital, Sanya, China.
Xiangqing WangDepartment of Neurology, The First Medical Center of Chinese PLA General Hospital, Beijing, China. bjxqwang13@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aimed to describe the changes in the etiology of adult epilepsy in different age groups over the past 25 years, with consideration of different time periods.

methodsA retrospective study was conducted using the clinical data of patients with adult-onset epilepsy at The First Medical Center of Chinese PLA General Hospital between February 1999 and March 2024.

resultsThe study included 5,712 patients from 25 provinces and 4 municipalities in China. The study found that the prevalence of unknown etiology has decreased overall, particularly after 2015, and that the proportion of epilepsy cases caused by metabolic etiologies has declined since 2016. However, since 2021, there has been an increase in immune-related epilepsy. The proportion of patients with structural epilepsy ranged from 29.7% to 90% across all age groups. Among epilepsy patients aged ≥ 51 years, structural epilepsy was predominant, accounting for the majority of cases. In particular, the proportion of epilepsy attributable to cerebrovascular disease increased with age at onset. With regard to gender, structural epilepsy was more common in males than in females.

conclusionsThis study highlights observed trends and changes in clinical diagnosis in epilepsy etiologies, revealing an obvious decrease in unknown etiology. The recent rise in immune-related epilepsy underscores the need for increased clinical vigilance. The observed gender and age disparities in structural epilepsy, particularly cerebrovascular-related cases in elderly males, provide critical insights for targeted preventive and therapeutic strategies.

Indexed as

Cerebrovascular DisordersEpilepsyAdolescentAdultAgedAged, 80 and overAge of OnsetChinaFemaleHumansMaleMiddle AgedPrevalenceRetrospective StudiesYoung AdultAdult-onsetEpilepsyEtiology

Identifiers

PMID41444553
PMCPMC12729239

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